Canonical Allele Identifier: PA2826636255
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791805
ClinVar RCV Id: RCV002450622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile523Leu
CA346754132
NM_001281494.2:c.1567A>C